Abstract

BackgroundCartilage injury and pathological degeneration are reported in millions of patients globally. Cartilages such as articular hyaline cartilage are characterized by poor self-regeneration ability due to lack of vascular tissue. Current treatment methods adopt foreign cartilage analogue implants or microfracture surgery to accelerate tissue repair and regeneration. These methods are invasive and are associated with the formation of fibrocartilage, which warrants further exploration of new cartilage repair materials. The present study aims to develop an injectable modified gelatin hydrogel.MethodThe hydrogel effectively adsorbed proteoglycans secreted by chondrocytes adjacent to the cartilage tissue in situ, and rapidly formed suitable chondrocyte survival microenvironment modified by ε-poly-L-lysine (EPL). Besides, dynamic covalent bonds were introduced between glucose and phenylboronic acids (PBA). These bonds formed reversible covalent interactions between the cis−diol groups on polyols and the ionic boronate state of PBA. PBA-modified hydrogel induced significant stress relaxation, which improved chondrocyte viability and cartilage differentiation of stem cells. Further, we explored the ability of these hydrogels to promote chondrocyte viability and cartilage differentiation of stem cells through chemical and mechanical modifications.ResultsIn vivo and in vitro results demonstrated that the hydrogels exhibited efficient biocompatibility. EPL and PBA modified GelMA hydrogel (Gel-EPL/B) showed stronger activity on chondrocytes compared to the GelMA control group. The Gel-EPL/B group induced the secretion of more extracellular matrix and improved the chondrogenic differentiation potential of stem cells. Finally, thus hydrogel promoted the tissue repair of cartilage defects.ConclusionModified hydrogel is effective in cartilage tissue repair.

Highlights

  • Articular cartilage defect and subchondral bone degeneration of the knee joint are prevailing clinical conditions associated with knee joint dysfunction, severe pain, and disability in some cases [1]

  • EPL and phenylboronic acids (PBA) modified Gelatin methacrylamide (GelMA) hydrogel (Gel-EPL/B) showed stronger activity on chondrocytes compared to the GelMA control

  • We evaluated the interaction between glucose and phenylboronic acids (PBA) through mechanical approaches as a reversible covalent interaction between cis-diol groups on polyols and ionic boronate state of PBA [30]

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Summary

Introduction

Articular cartilage defect and subchondral bone degeneration of the knee joint are prevailing clinical conditions associated with knee joint dysfunction, severe pain, and disability in some cases [1]. Modifications of the surface chemistry of material were found to affect the quantity and type of adsorbed protein [5], mesenchymal stem cell (MSC) adhesion, morphology, and the differentiation potential [6]. The study demonstrated that the nascent protein can be deposited within a day, thereby masking interfacial chemical interaction of the hydrogel. This affects the differentiation behavior of cells for several weeks. This study explored a cellular niche with in situ high adsorptions of extracellular matrix protein and glycosaminoglycan to improve the viability of native chondrocytes and the differentiation of MSCs. Cartilage injury and pathological degeneration are reported in millions of patients globally. The present study aims to develop an injectable modified gelatin hydrogel

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